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Osteogenic differentiation of bone mesenchymal stem cells regulated by osteoblasts under EMF exposure in a co-culture system 总被引:1,自引:0,他引:1
This study examined the osteogenic effect of electromagnetic fields (EMF) under the simulated in vivo conditions. Rat bone marrow mesenchymal stem cells (BMSCs) and rat osteoblasts were co-cultured and exposed to 50 Hz, 1.0 mT EMF for different terms. Unexposed single-cultured BMSCs and osteoblasts were set as controls. Cell proliferation features of single-cultured BMSCs and osteoblasts were studied by using a cell counting kit (CCK-8). For the co-culture system, cells in each group were randomly chosen for alkaline phosphatase (ALP) staining on the day 7. When EMF exposure lasted for 14 days, dishes in each group were randomly chosen for total RNA extraction and von Kossa staining. The mRNA expression of osteogenic markers was detected by using real-time PCR. Our study showed that short-term EMF exposure (2 h/day) could obviously promote prolifera- tion of BMSCs and osteoblasts, while long-term EMF (8 h/day) could promote osteogenic differen- tiation significantly under co-cultured conditions. Under EMF exposure, osteogenesis-related mRNA expression changed obviously in co-cultured and single-cultured cells. It was noteworthy that most osteogenic indices in osteoblasts were increased markedly after co-culture except Bmp2, which was increased gradually when ceils were exposed to EMF. Compared to other indices, the expression of Bmp2 in BMSCs was increased sharply in both single-cultured and co-cultured groups when they were exposed to EMF. The mRNA expression of Bmp2 in BMSCs was approximately four times higher in 8-h EMF group than that in the unexposed group. Our results suggest that Bmp2-mediated cellular interaction induced by EMF exposure might play an important role in the osteogenic differ- entiation of BMSCs. 相似文献
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本文探讨了我省淮河上游洪水型钩体病流行区,自1981年该地人群停止钩体菌苗预防接种后,加强防治知识的宣传教育,传染源的管理,群众实施堆肥发酵,改变散放为圈猪积肥,猪的圈养率达8113%,减少猪之间相互感染,猪钩体带菌率由70年代的876%降为189%〈4/212〉P<0.01;人群隐性感染率由2235%也降为194%P<0.01。改变猪散放为圈养的饲养方式,是行之有效的控制传染源的措施,从而控制本病的发生和流行 相似文献
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科学灭鼠控制出血热发病霍邱卫生防疫站(237400)魏强刘明宋明宇许中安陈家新丁广修我县是安徽省流行性出血热发病稳定的老疫区,1991年因特大洪涝灾害,生态环境遭受严重破坏,鼠密度和出血热发病持续增高,据姜家湖乡临闸村监测,室内鼠密度达10.0%,室... 相似文献
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目的 探讨不同浓度地塞米松(dexamethasone,DEX)作用不同时间对骨髓间充质干细胞(bone marrow mesenchymal stem cells,BMSCs)的增殖及成骨、成脂分化的影响.方法 体外分离培养大鼠BMSCs,将状态良好的第三代细胞接种于96孔板中,随机分组为对照组(不加入DEX)及不同浓度(1 nmol/L、10 nmol/L、0.1μmol/L、1μmol/L)DEX作用组,培养1、3、5、7、9 d后,分别用细胞增殖检测(CCK-8)法检测细胞增殖状况.将BMSCs接种于6孔板中,随机分为对照组及不同浓度(1 nmol/L、10 nmol/L、0.1μmol/L、1μmol/L)DEX作用组,培养7、14 d后分别用荧光定量PCR方法检测成骨、成脂相关基因的表达,培养14 d后用Western blot检测成骨、成脂相关蛋白的表达.培养5 d后进行碱性磷酸酶(alkaline phosphatase,ALP)染色,培养14 d后进行油红"O"染色、茜素红染色.结果 较低浓度的DEX促进BMSCs增殖,而较高浓度DEX抑制BMSCs增殖.干预早期,较低浓度的DEX促进BMSCs成骨分化而高浓度DEX抑制其成骨分化;干预晚期,各浓度DEX均促进BMSCs成骨指标的表达,但是不能诱导BMSCs钙质沉积.DEX浓度依赖性地促进BMSCs成脂相关指标基因和蛋白的表达,并诱导BMSCs细胞内脂质沉积.结论 DEX可直接影响BMSCs增殖及向成骨、成脂方向分化,这种效应存在浓度和干预时间依赖性. 相似文献
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采用ELISA、IFA检测特异性抗体,MCPENT检测中和抗体和HI,进行血清学分型。结果:选择姬鼠型疫区,接种沙鼠肾细胞Ⅰ型灭活出血热疫苗安全性较好。免疫后42天HFRS.V.IgG抗体阳性率为9643%,GMT=3518,180天有明显下降,加强免疫两周后阳性率达100%,而且1200天仍有3636%人群存在1∶10(+)抗体;MCPENT抗体较IFA抗体阳性率低,但疫苗免疫人群具有特异性回忆反应。中期流行病学防病效果接种组发病率为235/10万,对照组为4293/10万,保护率9453%。 相似文献
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目的观察共培养条件下电磁场干预对大鼠成骨细胞及骨髓间充质干细胞(MSCs)成骨定向分化的影响,并探讨电磁场促进成骨分化的相关机制。 方法体外分离培养SD大鼠BMSCs及成骨细胞,将第三代成骨细胞与BMSCs通过transwell培养小室建立共培养系统。采用随机数字表法将共培养细胞分为共培养组及共培养暴磁组,另随机选择单细胞培养的BMSCs及成骨细胞纳入单细胞培养组。共培养暴磁组细胞每日给予电磁场刺激4 h。于实验进行14 d后随机提取各组细胞总RNA,采用荧光定量PCR技术检测各组细胞Runx2、Sp7、碱性磷酸酶、I型胶原、骨形态形成蛋白-2及骨钙素基因表达情况,并选用茜素红染色法检测各组细胞矿化钙结节形成情况。 结果单细胞培养模式下BMSCs及成骨细胞其各项成骨相关基因表达水平均较低,而共培养模式下BMSCs及成骨细胞其各项成骨相关基因表达均呈现不同程度增强,并且以共培养暴磁组成骨细胞上述指标增强幅度较显著。通过茜素红染色发现,与单纯共培养组比较,共培养暴磁组细胞矿化钙结节数量明显增多。 结论低频电磁场干预可显著促进共培养条件下BMSCs及成骨细胞成骨定向分化,其可能机制为电磁场刺激能促进骨形态形成蛋白-2表达,使其通过自分泌或旁分泌方式介导细胞间信号转导,从而诱导BMSCs向成骨细胞分化及成骨细胞进一步成熟分化。 相似文献
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1991年我县遭受了百年不遇的特大洪涝灾害,全县10个区镇,54个乡镇,626个行政村,29万户,121万人遭受特大洪涝灾害,直接经济损失13.5亿元。洪水围困期间,迁移到淮河大堤及沿岗地区的人畜禽共居又高度集中,水源污染严重,环境卫生恶劣,加上盛夏酷暑, 相似文献